Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants-Reference-Cited by-同舟云学术

Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants

Published:2014-05 Issue:5 Volume:35 Page:1212.e7-1212.e10
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Bertolin Cinzia,D'Ascenzo Carla,Querin Giorgia,Gaiani Alessandra,Boaretto Francesca,Salvoro Cecilia,Vazza Giovanni,Angelini Corrado,Cagnin Annachiara,Pegoraro Elena,Sorarù Gianni,Mostacciuolo Maria Luisa

Funder

Association Française contre les Myopathies

ASLA onlus

Telethon-Italy

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference24 articles.

1. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?;Andersen;Nat. Rev. Neurol.,2011

2. Proposed criteria for familial amyotrophic lateral sclerosis;Byrne;Amyotroph. Lateral Scler.,2011

3. Genetic counselling in ALS: facts, uncertainties and clinical suggestions;Chiò;J. Neurol. Neurosurg. Psychiatry,2013

4. Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene;Chiò;Arch. Neurol.,2011

5. Extensive genetics of ALS: a population-based study in Italy;Chiò;Neurology,2012

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Analysis of SOD1 and C9orf72 mutations in patients with amyotrophic lateral sclerosis in Antioquia, Colombia;Biomédica;2022-12-01

2. TARDBP mutations in a cohort of Italian patients with Parkinson’s disease and atypical parkinsonisms;Frontiers in Aging Neuroscience;2022-09-29

3. Common mutations of interest in the diagnosis of amyotrophic lateral sclerosis: how common are common mutations in ALS genes?;Expert Review of Molecular Diagnostics;2020-06-16

4. Amyotrophic lateral sclerosis due to a SOD1 mutation and X-linked recessive bulbospinal neuronopathy in a single family;Acta Neurologica Belgica;2019-03-16

5. FUS ALS-causative mutations impact FUS autoregulation and the processing of RNA-binding proteins through intron retention;2019-03-04